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The validity and feasibility of saliva melatonin in assessing perioperative rhythm: an exploratory study based on perioperative patients

The validity and feasibility of saliva melatonin in assessing perioperative rhythm: an exploratory study based on perioperative patients

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070470
Enrollment
Unknown
Registered
2023-04-13
Start date
2023-04-13
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Circadian rhythm disturbance

Interventions

case series:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. American Society of Anesthesiologists (ASA) Levels I to III; 3. Return to the general ward after surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with Parkinson's disease, dementia (including dementia caused by Parkinson's disease, Alzheimer's disease and dementia with Lewy bodies) or mental illness; 2. Patients who are unable to communicate due to severe audio-visual impairments, language barriers and/or communication difficulties; 3. Alcohol dependence and drug addiction; 4. Oral diseases; 5. Shift workers; 6. Unexpected discharge or refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
plasma melatonin level;saliva melatonin level;

Secondary

MeasureTime frame
sleep quality;the intensity of pain at rest and with movement;body temperature;blood pressure;anxiety; depression;plasma cortisol level;saliva cortisol level;

Countries

China

Contacts

Public ContactLi Zhengqian

Peking University Third Hospital

zhengqianli@bjmu.edu.cn+86 180 0129 8582

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026